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2,6-diphenyl-3-dimethylaminomethylpyridine is a complex organic compound characterized by its unique molecular structure. It features a pyridine ring, which is a six-membered aromatic ring containing one nitrogen atom, with two phenyl groups attached at the 2nd and 6th positions. The 3rd position of the pyridine ring is occupied by a dimethylaminomethyl group, which consists of a nitrogen atom bonded to two methyl groups and a methylene group. 2,6-diphenyl-3-dimethylaminomethylpyridine is known for its potential applications in various chemical and pharmaceutical industries, particularly as a building block for the synthesis of more complex molecules. Its specific properties, such as solubility and reactivity, can be influenced by the presence of the phenyl and dimethylaminomethyl groups, making it a versatile component in organic synthesis.

5276-39-1

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5276-39-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5276-39-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,7 and 6 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5276-39:
(6*5)+(5*2)+(4*7)+(3*6)+(2*3)+(1*9)=101
101 % 10 = 1
So 5276-39-1 is a valid CAS Registry Number.

5276-39-1Downstream Products

5276-39-1Relevant academic research and scientific papers

AMINOMETHYLATION OF 1,5-DIPHENYL-1,5-PENTANEDIONE

Petrosyan, L.M.,Gevorgyan, G.A.,Engoyan, A.P.,Mndzhoyan, O.L.

, p. 551 - 554 (2007/10/02)

The result from the aminomethylation of 1,5-diphenyl-1,5-pentanedione is affected significantly both by the character of the amine component and by the medium.The products can be the monoaminomethyl derivative, the bisaminomethyl derivative, the substitut

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